Observable Hysteresis at Low Temperature in “Hysteresis Free

Jul 21, 2015 - In this paper we address the JV hysteresis behavior of planar organic–inorganic lead halide perovskite solar cells fabricated using P...
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Observable Hysteresis at Low Temperature in ‘Hysteresis Free’ Organic-Inorganic Lead Halide Perovskite Solar Cells Daniel Bryant1,2*, Scot Wheeler1, Brian C. O’Regan2, Trystan Watson2, Piers R. F. Barnes3, Dave Worsley2 and James Durrant1,2 * 1. Department of Chemistry and Centre for Plastic Electronics, Imperial College London, London SW7 2AZ 2. SPECIFIC, College of Engineering, Swansea University, Baglan Bay Innovation and Knowledge Centre, Central Avenue, Baglan, SA12 7AX 3. Physics Department, Imperial College—London, London, United Kingdom, SW7 2AZ AUTHOR INFORMATION Corresponding Author *Email

addresses: [email protected], [email protected]

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Abstract

In this paper we address the JV hysteresis behaviour of planar organic-inorganic lead halide perovskite solar cells fabricated using PC60BM as the cathode. At room temperature, these devices exhibit apparently hysteresis free JV scans. We observe that cooling the temperature to 175K results in the appearance of substantial JV hysteresis. Employing chronoamperometric measurements, we demonstrate that the half-time for the relaxation process underlying this hysteresis slows from 0.6 s at 298K to 15.5 s at 175K, yielding an activation energy of 0.12 eV. We further demonstrate that by cooling a cell to 77K whilst held under positive bias, we are able to ‘freeze’ the cell into the most favourable condition for efficient photovoltaic performance. We thus conclude that changes to device architecture which appear to remove room temperature JV hysteresis may not remove the underlying process(es), but rather shift them to timescales not readily

observable

in

typical

room

temperature

JV

scans.

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Hybrid organic-inorganic lead halide perovskite photovoltaics offer the promise of inexpensive solar power generation from solution processed thin films. Solar power conversion efficiencies of 16-20% have been reported1-2 in a variety of configurations including dye-sensitised solar cell style architecture and planar hetrojunctions, in which the cathode is either at the bottom or top of the layer stack deposited on a transparent conducting oxide.3-5 Perovskite solar cells fabricated with methyl ammonium lead iodide CH3NH3PbI3 (MAPI) as the photoactive layer often exhibit hysteresis in their photovoltaic properties. Depending upon the scan speed, this can result in overestimation of the power conversion efficiency evaluated from the photocurrent as the voltage is swept from forward bias (FB) to reverse bias (RB) as opposed to determination from the steady state photocurrent at the maximum power point (mpp).6-8 Recently, several groups have demonstrated approaches to produce MAPI solar cells with apparently negligible hysteresis in the JV curves at room temperature. For example MAPI-Cl based cells in which a transparent conducting oxide cathode is coated with a thin (200nm) mesoporous TiO2 layer covered with a self-assembled monolayer of C60 molecules gave steady state power outputs similar to that inferred from a JV measurements and almost independent of factors such as scan speed and prebiasing.9-10 MAPI cells with contact layers commonly used in organic photovoltaic (OPV) cells such as poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS), Phenyl-C61butyric acid methyl ester (PCBM) and Lithium Fluoride (LiF) have also been reported not to show hysteresis effects under normal measurement conditions. Since the cathode is deposited on the top of the layer stack in these cells (similar to the standard configuration used organic photovoltaic devices) we will refer to this device architecture as fullerene top cathode cells. The reason for the apparent decrease in hysteresis, relative to devices where the MAPI is in contact with a metal oxide cathode at the bottom of the layer stack (‘bottom cathode’ architecture), is not

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fully understood. It has been suggested that fullerene molecules may play a role in passivating the MAPI interface.11-13 This paper is concerned with investigating the apparent absence of hysteresis effects in such fullerene top cathode MAPI solar cells. From an engineering point of view, cells that show no hysteresis at room temperature represent a significant improvement and a step towards commercialisation. However it is not apparent whether the use of the fullerene contact layers between the MAPI and the cathode has removed/reduced the magnitude of the underlying causes of hysteresis, or alternatively, whether the timescale of hysteresis has changed. If devices equilibrate on a time scale that is too fast to be resolved using typical JV measurement then they would appear hysteresis free. Here, we investigate this possibility by cooling MAPI solar cells with fullerene top cathode architectures below room temperature to observe whether hysteresis can be identified in devices where the thermally activated kinetic processes have been slowed. We show that at lower temperatures the nominally ‘hysteresis free’ devices do show significant hysteresis, and we investigate the kinetics of the relaxation of the photovoltaic properties to equilibrium to elucidate the origins of this phenomenon.

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Figure 1. JV curves obtained under simulated 1 sun illumination for a fullerene top cathode MAPI cell in a sweep direction from FB-RB (solid line) and RB-FB (dashed line) at a) room temperature (293K) and b) at temperatures ranging between 77-293K at scan speeds of 0.125 V/s. A schematic of the cell is shown as an inset to (a).

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Cells were fabricated according to a previously reported method to give fullerene top cathode cells consisting of planar layers of PEDOT:PSS, CH3NH3PbI3 (MAPI) and PC60BM, as shown in Figure 1a inset. The room temperature JV curves in Figure 1a show near identical performance when scanning from FB-RB and from RB-FB at a rate of 0.125 V/s. These cells do not display the hysteresis typically observed in metal oxide bottom cathode architectures, as shown in Figure S1. Even when the scan rate is increased from 0.125V/s to 4.75V/s (Figure S2) there is little change in the JV curves, consistent with previous reports.11 The photovoltaic performance data as a function of scan speed is presented in Table S1. In particular, for the fullerene top cathode device, the degree of hysteresis metric (DoH), as defined by Equation S1, 7 showed a minor increase from 0.013 to 0.062 with increasing scan speed. This is in contrast to MAPI cells with metal oxide bottom cat architectures, where much larger DoH values are seen.7 The observation of a marginal increase in the DoH with increasing scan speed in our fullerene top cathode cells could suggest the presence of a hysteresis effect in the device that is hard to quantify at easily accessible JV scan speeds. We now turn to temperature dependent measurements. Fullerene top cathode devices cells were kept under vacuum in a cryostat to avoid cell degradation and water vapour condensing onto the cells at low temperatures. Cells were allowed to equilibrate at each temperature in the dark at open circuit for 20 minutes before measurement. Figure 1c shows a clearly observable hysteresis for all measurements below room temperature, even at the lowest scan speed of 0.125 V/s used in this study. The FB-RB JV sweeps (solid lines) show a significantly higher short ciruit photocurrent relative to the RB-FB sweeps (dashed lines). Table S2 summarises the solar cell performance parameters derived from these JV curves, including the degree of hysteresis, which varies significantly from 0.13 to 0.659 as the temperature is lowered to 175K. At 77K the

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photovoltaic performance of the cell in greatly reduced; however the cells using this sweep rate show a reduced hysteresis with a degree of hysteresis of 0.115. In order to confirm the effect observed is a property of the perovskite based cells, and not an artefact of the cell architecture or measurement procedure, we performed the same experiments on a standard organic PV (OPV) cell. The key difference between the two cells was that the MAPI perovskite layer was replaced with the well-studied polymer: fullerene blend PCDTBT: PCBM. Figure S3 shows the JV characteristics of this OPV cell at 175K. While the performance of this device is reduced (primarily due to resistance losses as reported in reference14), the cell shows no sign of hysteresis.

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Figure 2. a) Current density of a fullerene top cathode MAPI cell plotted as a function of time, after +1.2V pre-biasing conditions in the dark for 3 minutes (grey shaded area) and thenswitching to short circuit current conditions whilst simultaneously illuminating the cell

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under 1 sun intensity at different temperatures. b) Activation energy analysis of the temperature dependence of the decay half times obtained from the curves in (a). The JV curves indicate that a hysteresis effect is still present within these fullerene top cathode cells. In such JV scans, it is difficult to decouple the effects of both voltage and time as these are changing simultaneously. It has been shown previously that chronoamperometry can be employed to separate the effects of the response of perovskite devices to a change in voltage from its relaxation with time, and thereby interrogate in more detail the underlying process(es) causing the hysteresis observed in the JV scans. To undertake such experiments, the cell was held at a fixed forward bias of +1.2V for 3 minutes in the dark before being illuminated at 1 sun equivalent intensity with white LEDs and simultaneously switched to short circuit. Following the synchronous switch to short circuit and illumination, the short circuit photocurrent (J sc) in the device relaxes towards a steady state condition, allowing the relaxation processes underlying the hysteresis observed in the JV data to be quantified in terms of a time constant and magnitude as discussed previously. Photocurrent decays from the fullerene top cathode device measured at different temperatures (ranging from 175 – 293 K) can be seen in Figure 2a. Two things are immediately obvious from the curves. Firstly it is apparent that the relaxation time for J sc to reach steady state increases as the temperature decreases, with decay half times ranging from 0.6 to 15.5 seconds as the temperature decreases from 293K to 175K. The other observation is that whilst the initial short circuit photocurrent is independent of temperature, the magnitude of the loss of photocurrent resulting from the relaxation process increases as the temperature is decreased. In order to study the kinetics of the relaxation process, half-times for the decay were obtained and plotted in Figure 2b. It is apparent that the relaxation rate of decay follows

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Arrhenius behaviour over the temperature range investigated, with an activation energy of 0.12 ±0.02eV.

Figure 3. a) Current density of a fullerene top cathode MAPI solar cell plotted as a function of time when under different pre-biasing conditions in the dark for 3 minutes (grey shaded area) and then switching to short circuit current conditions whilst simultaneously illuminating the cell under 1 sun intensity at 293 K. b) same as (a) but expanded to only see the 10 seconds around the light is turn on. c) same as (a) however with the cell held at 175K. d) same as (a) but with a bottom cathode MAPI cell contacted with TiO2 and Spiro-OMeTAD.

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To investigate further the effect of relaxation process(es) underlying the JV hysteresis, we undertook additional chronoamperometry measurements as for Figure 2, but holding the cells at a range of initial voltages (‘pre-bias’ voltages) prior to switching to short-circuit under irradiation, for fullerene top cathode cells either held at room temperature or 175K. The results at room temperature are shown in Figure 3a, with the corresponding time expansion in figure 3b. It is apparent that whilst for forward pre-biases, the relaxation results in a decay of the observed photocurrent, for reverse pre-biases, the relaxation results in an increase in observed photocurrent. In all cases, the steady state currents tend towards the same value. We also note the kinetics of the relaxation process differ with pre-bias, and in some cases show clearly biphasic, and behaviour of opposite signs, clearly indicating that at least two different processes on different timescales cause this relaxation. Qualitatively similar behaviour is observed at 175 K, although on slower timescales, as shown in Figure 3c. It is instructive to compare these data against analogous room temperature data for a conventional bottom cathode cell comprising of ITO/TiO2 compact layer/MAPI/Spiro-OMeTAD/Au as shown in Figure 3d. It is apparent that the relaxation data collected for this conventional MAPI at room temperature is strikingly similar to the data collected for the fullerene top cathode cell measured at 175 K.

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Figure 4. JV curves taken of a MAPI fullerene top cathode solar cell at 77K as a function of different biasing conditions whilst cooling from room temperature down to 77K. Data shown for bothsweep directions at a scan speed of 0.125 V/s. Since pre-biasing clearly affects the state of the cell and its current / voltage behaviour, we attempted to ‘freeze’ in this conditioning in the cell by biasing the cell in the dark whilst cooling it down from room temperature to liquid nitrogen temperatures (77K). Figure 4 shows that when no bias, or a reverse bias, is applied and the cell is cooled down, the JV performance of the cell is poor, whereas when the cells are cooled down under a forward bias of 1.2V the cells show superior, stable JV performance even after this forward bias has been removed. The smaller amount of hysteresis in these 77 K data is believed to come from the process causing hysteresis being slowed down at 77 K to a timescale significantly slower than the scan time. From this observation we conclude that at room temperature with no external bias in the dark these cells are not in a state that is optimal for JV performance. However under illumination or when a

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forward external bias is applied the cell equilibrates to a condition whereby it gives an increased photovoltaic performance. By cooling the cell whilst under forward bias, we are able to essentially ‘lock in’ this favourable condition, or more specifically extend the time it is in this condition to beyond the experiment timescale, resulting in improved performance at 77 K. We have shown the relaxation processes which cause JV hysteresis in many MAPI perovskite solar cells are still present even in fullerene top cathode cells which show no apparent hysteresis in JV scans at room temperature. Hysteresis behaviour is observed in these fullerene top contact cells at lower temperatures, shown to be due to the time scale of the relaxation process causing the hysteresis to slow down to the same timescale as the scan speed. Significant hysteresis in the JV scan is only observed if the timescale of the relaxation process causing the hysteresis is similar to the timescale of the JV scan. Such apparent relaxation processes may at least in part be associated with capacitive charging / discharging currents, as has been discussed previously.16 For fullerene top cathode devices it was seen at room temperature this relaxation process has a decay half time from a forward bias condition to short circuit of 0.6 seconds which is faster than the total scan time (~20 s) scan speeds of 0.125 V/s. At lowered temperatures of 175K, the relaxation decay half time of 15.5 seconds is similar to typical scan times (~ 20 s), resulting in the observation of substantial hysteresis in the JV scan. At 77 K it appears that the relaxation process is slower than the scan speed employed, again resulting in little hysteresis behavior. Indeed extrapolation of the Arrhenius plot in Figure 2b would result in a half time of ~1700 seconds, well beyond the scan time. As such it is apparent that room temperature JV scans, whilst crucial to determining practical device operational efficiency, are of only limited effectiveness in determining the presence of the underlying processes which can cause JV hysteresis.

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It is interesting to note that at 293 K, Figure 1 indicates that the stabilised photocurrent in our fullerene top cathode MAPI cells is ~ 20mA/cm2 . Figure 3a shows that following a positive pre-bias, the photocurrent is initially Jsc = 25 mA/cm2 but then rapidly decays with a ~ 0.6 s halftime to a steady state value of 20 mA/cm2. At lower temperatures the magnitude of this decay is greater, falling from an initial value of 25 mA /cm2 to 16 mA/cm2 in the case of a cell at 175K. This raises the possibility that if cells could be stabilised under the conditions achieved by forward bias, then it may be possible to extract significantly higher photocurrents, and therefore potentially higher device efficiencies. In this regard, it is noted that ‘freezing’ the cells under forward bias conditions, as shown in Figure 4 at 77K, results in a significant enhancement in short circuit photocurrent and device efficiency. From Figure 3a, it is apparent that fullerene top cathode MAPI cells reach equilibrium on a much faster timescale than that seen with other perovskite PV architectures and contacts. The value obtained for the activation energy in Figure 3b of 0.12 eV is significantly lower than that previously reported for MAPI devices with a bottom cathode architecture

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halide (I and Br) perovskite solar cell contacted with Spiro-OMeTAD and compact TiO2 which showed significant hysteresis at room temperature.18 The lower activation energy measured herein may be related to our observation of faster relaxation kinetics. This change in activation energy suggests that this particular cell architecture, and in particular the inclusion of the PEDOT:PSS and PC60BM interlayers, has accelerated the timescale of the process(es) causing the hysteresis effect. This may be related to PC60BM passivation effects discussed previously.11 However it has also recently been shown that the value of activation energy for organic-inorgaic lead halide perovskite can be a function of light intensity and measurement temperature range. 19 We also note that our chronoamperometry studies provide clear evidence for biphasic relaxation

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kinetics, suggesting at least two processes may be contributing to overall JV hysteresis. Detailed analysis of this biphasic behaviour is beyond the scope of this paper, but may be related to the observation of different activation energies for the processes underlying JV hysteresis determined from different studies. In any case, whilst there is extensive evidence that the observation of JV hysteresis is associated with relaxation processes with the MAPI light absorber induced by applied voltages, it is apparent that the timescale of these relaxation processes can be strongly dependent upon the details of solar cell device architecture and/or contact materials.

ASSOCIATED CONTENT Supporting Information. Details of fabrication methods for fabrication and measurement techniques used within this study can be found within the supporting information. As well as JV and cell performance data referred to within the text. This material is available free of charge via the Internet at http://pubs.acs.org AUTHOR INFORMATION Corresponding Author Email addresses: [email protected], [email protected] ACKNOWLEDGMENT Funding from the EPSRC EP/IO1927B/1, EP/J002305/1 and EP/M014797/1 is gratefully acknowledged. We also thank Pabitra Tuladhar and Xiaoe Li for assistance with device fabrication facilities

REFERENCES

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(1)

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Nie, W.; Tsai, H.; Asadpour, R.; Blancon, J-C.; Neukirch, A.J.; Gupta, G.; Crochet, J. J.; Chhowalla, M.; Tretiak, S.; Alam, M. A.; et al. High-Efficiency Solution-Processed Perovskite Solar Cells With Millimeter-Scale Grains. Science. 2015, 347, 522-525

(2)

Jeon, N. J.; Noh, J. H.; Yang, W. S.; Kim, Y. C.; Ryu, S.; Seo, J.; Seok, S. I. Compositional Engineering of Perovskite Materials For High-Performance Solar Cells. Nature. 2015, 517, 476– 480

(3)

Burschka, J.; Pellet, N.; Moon, S.-J.; Humphry-Baker, R.; Gao, P.; Nazeeruddin, M. K.; Gratzel, M. Sequential Deposition as a Route to High-Performance Perovskite-Sensitized Solar Cells. Nature. 2013, 499, 316– 319

(4)

Liu, D.; Kelly, T. L.; Perovskite Solar Cells With A Planar Heterojunction Structure Prepared Using Room-Temperature Solution Processing Techniques. Nat. Photon. 2014, 8, 133–138.

(5)

Malinkiewicz, O.; Yella, A.; Lee, Y. H.; Minguez Espallargas, G.; Graetzel, M.; Nazeeruddin, M. K.; Bolink, H. J. Perovskite Solar Cells Employing Organic ChargeTransport Layers. Nat. Photon. 2014, 8, 128– 132.

(6)

Snaith, H. J.; Abate, A.; Ball, J. M.; Eperon, G. E.; Leijtens, T.; Noel, N. K.; Stranks, S. D.; Wang, J. T.-W.; Wojciechowski, K.; Zhang, W. Anomalous Hysteresis in Perovskite Solar Cells. J. Phys. Chem. Lett. 2014, 5, 1511– 1515.

(7)

Sánchez, R. S.; Gonzalez-Pedro, V.; Lee, J.-W.; Park, N.-G.; Kang, Y. S.; Mora-Sero, I.; Bisquert, J. Slow Dynamic Processes in Lead Halide Perovskite Solar Cells. Characteristic Times and Hysteresis. J. Phys. Chem. Lett. 2014, 5, 2357– 2363

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(8)

Tress, W.; Marinova, N.; Moehl, T.; Zakeeruddin, S.M.; Nazeeruddin, M.K.; Grätzel, M.; Understanding The Rate-Dependent J–V hysteresis, Slow Time Component, and Aaging in CH3NH3PbI3 Perovskite Solar Cells: The Role Of A Compensated Electric Field. Energ. Envi. Sci. 2015, 8, 995-1004.

(9)

Jeon, N. J.; Noh, J. H.; Kim, Y. C.; Yang, W. S.; Ryu, S.; Seok, S. I. Solvent Engineering for High-Performance Inorganic–Organic Hybrid Perovskite Solar Cells. Nat. Mater. 2014, 13, 897– 903

(10) Wojciechowski, K.; Stranks, S.; Abate, A.; Sadoughi, G.; Sadhanala, A.; Kopidakis, N.; Rumbles, G.; Li, C.; Friend, R.; Jen, A. Heterojunction Modification For Highly Efficient Organic–Inorganic Perovskite Solar Cells. ACS. Nano. 2014, 8, 12701– 12709 (11) Shao, Y.; Xiao, Z.; Bi, C.; Yuan, Y.; Huang, J. Origin and Elimination Of Photocurrent Hysteresis by Fullerene Passivation in CH3NH3PbI3 Planar Heterojunction Solar Cells Nat. Commun. 2015, 5, 5784 (12) Lin, Q.; Armin, A.; Nagiri, R. C. R.; Burn, P. L.; Meredith, P. Electro-Optics of Perovskite Solar Cells. Nat. Photon. 2014, 9, 106– 112 (13) Seo, J. W.; Park, S.; Kim, Y. C.; Jeon, N. J.; Noh, J. H.; Yoon, S. C.; Seok, S. I. Benefits of Very Thin PCBM and LiF Layer For Solution-Processed P-I-N Perovskite Solar Cells. Ener Environ. Sci. 2014, 7, 2642– 2646 (14) Street, R. A.; Schoendorf, M.; Roy, A.; Lee, J. H. Interface State Recombination in Organic Solar Cells. Phys. Rev. B. 2010, 81, 205307

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(15) O’Regan, B. C.; Barnes, P. R. F.; Li, X.; Law, C.; Palomares, E.; Marin-Beloqui, J. M. Opto-Electronic Studies of Methylammonium Lead Iodide Perovskite Solar Cells with Mesoporous TiO2: Separation of Electronic and Chemical Charge Storage, Understanding Two Recombination Lifetimes, and the Evolution of Band Offsets During J–V Hysteresis. J. Am. Chem. Soc. 2015, 137, 5087–5099 (16) Almora, O.; Zarazua, I.; Mas-Marza, E.; Mora-Sero, I.; Bisquert, J.; Garcia-Belmonte,G. Capacitive Dark Currents, Hysteresis, and Electrode Polarization in Lead Halide Perovskite Solar Cells. J. Phys. Chem. Lett. 2015, 6, 1645– 1652 (17) Eames, C.; Frost, J. M.; Barnes, P. R. F., O’Regan, B. C.; Walsh, A.; Islam, M. S. Ionic Transport in Hybrid Lead Iodide Perovskite Solar Cells. Nat. Comm. 2015, 6, 7497, (18) Hoke, E. T.; Slotcavage, D. J.; Dohner, E. R.; Bowring, A. R.; Karunadasa, H. I.; McGehee, M. D.Reversible Photo-Induced Trap Formation in Mixed-Halide Hybrid Perovskites for Photovoltaics. Chem. Sci. 2014, 6, 613– 617 (19) Yuan, Y.; Chae, J.; Shao, Y.; Wang, Q.; Xiao, Z.; Centrone, A.; Huang, J.; Photovoltaic Switching Mechanism in Lateral Structure Hybrid Perovskite Solar Cells. Adv. Ener. Mat. 2015, 10.1002/aenm.201500615

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